| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303652-177303989 | Common:8; Rare:222 | ||||
| chr5:177311862-177312054 | Common:2; Rare:93 | ||||
| chr5:177312190-177312740 | Common:3; Rare:223 | ||||
| chr5:177351620-177351971 | Rare:177 | ||||
| chr5:177370580-177370940 | Common:2; Rare:226 | ||||
| chr5:177370930-177371200 | Common:37; Rare:248 | ||||
| chr5:177404360-177404710 | Common:2; Rare:135; Clinvar (benign):2 | ||||
| chr5:177426220-177426733 | Common:5; Rare:215 | ||||
| chr5:177446609-177446845 | Common:2; Rare:69 | ||||
| chr5:177447833-177448319 | Common:4; Rare:122 | ||||
| chr5:177466660-177467260 | Common:2; Rare:193 | ||||
| chr5:177473401-177474151 | Common:2; Rare:193 | ||||
| chr5:177496750-177497130 | Common:7; Rare:147 | ||||
| chr5:177497548-177497888 | Common:2; Rare:236 | ||||
| chr5:177516875-177517100 | Common:4; Rare:165; Clinvar:2; Clinvar (pathogenic):2 |